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Stability of Contemporary Knee Arthroplasty

Primary Purpose

Knee Osteoarthritis

Status
Active
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Medacta International, GMK Sphere medially stabilized knee
Sponsored by
Oslo University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Knee Osteoarthritis focused on measuring Total Knee Arthroplasty (TKA), Total Knee Replacement (TKR), Kinematics, RSA, Knee arthroplasty, Implant stability, Migration, Wear, Medial pivot

Eligibility Criteria

50 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with knee osteoarthritis

Exclusion Criteria:

  • Preoperative severe deformity (Femoro-tibial angle < 175°or > 190°measured on a full-length leg image at weight bearing)
  • Preoperative flexion contracture more than 15°
  • Preoperative limited range of motion under anesthetics (less than 110°)
  • Less than 50 or more than 75 years of age at the time of surgery
  • Use of walking aids because of other musculoskeletal and neuromuscular problems
  • Preoperative diagnosis other than osteoarthritis and avascular necrosis (e.g. rheumatoid arthritis, tumors)
  • Revision arthroplasty
  • Obesity with BMI >35
  • Impaired collateral ligaments
  • Malposition of femoral and tibial implants (Internally rotated or more than 10° externally rotated implants will be excluded. The rotation of femoral implant is measured on postoperative CT images in reference to surgical epicondylar line. The rotation of tibial implant is determined according to Berger's measurement)
  • Postoperative revision surgery due to deep wound infection

Sites / Locations

  • Oslo University Hospital

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

GMK Sphere

Arm Description

Patients receive a GMK Sphere Total Knee Replacement.

Outcomes

Primary Outcome Measures

Stability of the GMK Sphere prosthesis measured by Radiostereometric Analysis (RSA)
Stability of the implant is measured in mm after 5 years (Maximum Total Point Motion in mm, MTPM)

Secondary Outcome Measures

Knee Society Score (KSS)
Patient reported outcome measures
Forgotten Joint Score 12 (FJS-12)
Patient reported outcome measures
Knee injury and Osteoarthritis Outcome Score (KOOS)
Patient reported outcome measures
Range of motion (ROM)
Clinical measurement using goniometer
Hip-knee-ankle angle (HKA-angle)
The axis of the lower extremity after knee arthroplasty
CT-rotation of implants
Evaluation of tibia implant rotation using Berger's method
Stability of the GMK Sphere prosthesis
Stability of the implant is measured in mm and degrees after 5 years using RSA (translation and rotasjon for x, y and z)

Full Information

First Posted
April 28, 2016
Last Updated
December 9, 2021
Sponsor
Oslo University Hospital
Collaborators
Helse More and Romsdal Trust, Medacta International SA
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1. Study Identification

Unique Protocol Identification Number
NCT02861794
Brief Title
Stability of Contemporary Knee Arthroplasty
Official Title
Evaluation of Early Migration of Medially Stabilized Arthroplasty as a Predictor of Long Time Survivorship (Implant Design Study)
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Active, not recruiting
Study Start Date
May 2016 (Actual)
Primary Completion Date
December 31, 2022 (Anticipated)
Study Completion Date
December 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oslo University Hospital
Collaborators
Helse More and Romsdal Trust, Medacta International SA

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Total joint replacement is an efficacious treatment for osteoarthritis of hips and knees. Both total knee replacement (TKR) and total hip replacements (THR) have excellent implant survivorship. However, patient satisfaction is lower in TKR than THR. A possible cause of the discrepancy is the unnatural knee kinematics after TKR. Various implants designs have been developed to solve the problem. However, most of their designs are based on experimental data and little has been studied about their actual performance in vivo. In this study, the investigators will analyze the in vivo stability of the Global Medacta Knee Sphere (GMK Sphere) implant. Migration of the implants will be monitored with a high precision measuring method called Radiostereometric Analysis (RSA). The investigators assume the investigators study will contribute the development of more satisfying knee implants.
Detailed Description
Worldwide the number of patients requiring treatment for osteoarthritis is increasing due to increasing obesity, an ageing population and a high demanding younger population. Learmonth describes hip arthroplasty as the "operation of the century" because patients are highly satisfied with pain relief and function after the procedure. Knee arthroplasties have in recent years also shown promising results and have surpassed hip arthroplasty in frequency in western countries. However, patient satisfaction is not as high. Reported problems are insufficient function and persistent pain. On the other hand, knee arthroplasties are increasingly implanted in younger and more active patients who require high function and quality of life. Improvement of knee implants is an urgent issue in the field of orthopaedic research. Knee Kinematics and implant designs A possible cause of lower function of replaced knees is the unnatural postoperative knee kinematics. Kinematics of replaced knees is closely related to their function. Studies show that replaced knees with excellent flexion angles have kinematic similarities to normal knees and malalignments of implants can cause postoperative pain. Compared to hip joints which are simple ball-and socket joints, the kinematics of knee joints is more complex. The kinematics are a combination of a rolling and gliding motion of the femoral condyles and rotation of the tibia. Based on the kinematics of the normal knee joint, various attempts have been made on the design of knee implants to reconstruct normal kinematics after replacement surgery. All of these implants have satisfying survivorship, but unicondylar arthroplasty which retains both cruciate ligaments has the best clinical results with survivorship at 15 years 93%. In total knee replacement (TKR) the Anterior Cruciate Ligament (ACL) and possibly the Posterior Cruciate Ligament (PCL) are sacrified. When sacrificing the one or both of the cruciate ligaments, natural knee kinematics are affected. The function of the cruciate ligaments can be mimicked by different designs of the tibial insert. The most used knee implant in Norway, the NexGen Cruciate-retaining (CR) implant design, does not retain the ACL and does not mimic natural knee kinematics. The tibial insert of the medial pivot implant design (GMK Sphere) has a constrained medial ball in socket joint and at the same time allows lateral anterioposterior movement. This new design was developed by a group of dedicated researchers. The design intention is to resemble the function of the cruciate ligaments and at the same time allow for lateral anterioposterior movement (rollback). Small alterations in implant design can influence the survival of implants. The final design of the GMK Sphere was introduced in 2012. New implants should be monitored and assessed in small, controlled trials with high precision measuring methods. Analytical Method RSA has been used in orthopedic research fields since 1970s. The original application of this method was for the evaluation of implant migration (i.e. fixation) and polyethylene wear of artificial joints using static X-ray pictures. Clinically relevant association between early migration of tibial implants detected by RSA and late revision for loosening has been reported. Also, attempts to measure in vivo polyethylene wear have been reported using RSA. Purpose of this study The aim of this study is to analyse the in vivo performance (e.g. stability) of a medially stabilized knee arthroplasty implant (Medacta International, GMK Sphere) using static RSA method over a period of 5 years. 2-year results have already been analysed and are inconclusive in regards to migration as the implant is apparently stable, but shows greater than anticipated movement. Mid-term follow-up (5-year) is therefore essential to evaluate migration of this implant. We therefore wish to obtain 5-year follow-ups of these patients. Additionally, the investigators will analyse the wear in the ball and socket (medial) side of the tibiofemoral articulation. 30 patients will go through stability and wear testing with static RSA. This study will contribute to the safety for patients with this new implant by providing basic knowledge of this knee arthroplasty and promoting further development of knee implant designs.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Osteoarthritis
Keywords
Total Knee Arthroplasty (TKA), Total Knee Replacement (TKR), Kinematics, RSA, Knee arthroplasty, Implant stability, Migration, Wear, Medial pivot

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Prospective interventional single group cohort study
Masking
None (Open Label)
Masking Description
Non-blind
Allocation
N/A
Enrollment
31 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
GMK Sphere
Arm Type
Other
Arm Description
Patients receive a GMK Sphere Total Knee Replacement.
Intervention Type
Procedure
Intervention Name(s)
Medacta International, GMK Sphere medially stabilized knee
Intervention Description
Total Knee Replacement
Primary Outcome Measure Information:
Title
Stability of the GMK Sphere prosthesis measured by Radiostereometric Analysis (RSA)
Description
Stability of the implant is measured in mm after 5 years (Maximum Total Point Motion in mm, MTPM)
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Knee Society Score (KSS)
Description
Patient reported outcome measures
Time Frame
5 years
Title
Forgotten Joint Score 12 (FJS-12)
Description
Patient reported outcome measures
Time Frame
5 years
Title
Knee injury and Osteoarthritis Outcome Score (KOOS)
Description
Patient reported outcome measures
Time Frame
5 years
Title
Range of motion (ROM)
Description
Clinical measurement using goniometer
Time Frame
5 years
Title
Hip-knee-ankle angle (HKA-angle)
Description
The axis of the lower extremity after knee arthroplasty
Time Frame
5 years
Title
CT-rotation of implants
Description
Evaluation of tibia implant rotation using Berger's method
Time Frame
5 years
Title
Stability of the GMK Sphere prosthesis
Description
Stability of the implant is measured in mm and degrees after 5 years using RSA (translation and rotasjon for x, y and z)
Time Frame
5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with knee osteoarthritis Exclusion Criteria: Preoperative severe deformity (Femoro-tibial angle < 175°or > 190°measured on a full-length leg image at weight bearing) Preoperative flexion contracture more than 15° Preoperative limited range of motion under anesthetics (less than 110°) Less than 50 or more than 75 years of age at the time of surgery Use of walking aids because of other musculoskeletal and neuromuscular problems Preoperative diagnosis other than osteoarthritis and avascular necrosis (e.g. rheumatoid arthritis, tumors) Revision arthroplasty Obesity with BMI >35 Impaired collateral ligaments Malposition of femoral and tibial implants (Internally rotated or more than 10° externally rotated implants will be excluded. The rotation of femoral implant is measured on postoperative CT images in reference to surgical epicondylar line. The rotation of tibial implant is determined according to Berger's measurement) Postoperative revision surgery due to deep wound infection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephan Maximillian Røhrl, MD, PhD
Organizational Affiliation
Center for Implant and Radiostereometric Research Oslo (CIRRO)
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Frank-David Oehrn, MD
Organizational Affiliation
Kristiansund Hospital, Helse More and Romsdal Trust
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Lars Harald William Engseth, MD, PhD
Organizational Affiliation
Center for Implant and Radiostereometric Research Oslo (CIRRO)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Oslo University Hospital
City
Oslo
ZIP/Postal Code
0470
Country
Norway

12. IPD Sharing Statement

Plan to Share IPD
No
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Stability of Contemporary Knee Arthroplasty

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